Colon Cancer: Gene >> ATIC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000236959
Start	215326122:215326122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766526084
CDS Mutation	c.515G>A
AA Mutation	p.Arg172His(p.R172H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000236959
Start	215326010:215326010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.403G>A
AA Mutation	p.Ala135Thr(p.A135T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000236959
Start	215326891:215326891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549649169
CDS Mutation	c.601G>A
AA Mutation	p.Val201Ile(p.V201I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000236959
Start	215349566:215349566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149999349
CDS Mutation	c.1690G>A
AA Mutation	p.Gly564Ser(p.G564S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000236959
Start	215349169:215349169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1579T>C
AA Mutation	p.Trp527Arg(p.W527R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000236959
Start	215326835:215326835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.545C>G
AA Mutation	p.Thr182Arg(p.T182R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000236959
Start	215346823:215346823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1385C>T
AA Mutation	p.Ala462Val(p.A462V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000236959
Start	215312549:215312549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.71T>C
AA Mutation	p.Leu24Pro(p.L24P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000236959
Start	215338816:215338816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199518893
CDS Mutation	c.1136G>A
AA Mutation	p.Arg379Gln(p.R379Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000236959
Start	215332428:215332428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556427086
CDS Mutation	c.735C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000236959
Start	215349604:215349604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750485941
CDS Mutation	c.1728C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000236959
Start	215349139:215349151(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1549_1561delGAGTTACTCACTG
AA Mutation	p.Glu517ArgfsTer11(p.E517Rfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000236959
Start	215326028:215326028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774939270
CDS Mutation	c.421C>T
AA Mutation	p.Arg141Ter(p.R141*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000236959
Start	215338815:215338815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200150457
CDS Mutation	c.1135C>T
AA Mutation	p.Arg379Ter(p.R379*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ATIC

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000236959
Start	215344790:215344790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1239T>A
Mutation Classification	Silent
Feature Type	Transcript